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5" Pointed Bone Clamp

FDA UDI

Class I (US FDA UDI)

by Biopro, Inc.

Identity

Trade Name
5" POINTED BONE CLAMP FDA UDI
Generic Name
Temporal bone holder FDA UDI
Model / Reference
18338 FDA UDI

Identifiers

Primary DI / UDI-DI
00810012485128 FDA UDI
510(k) Number
K083490 FDA UDI
FDA Product Code
HXD FDA UDI
GMDN Term
Temporal bone holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Temporal bone holder

5" Pointed Bone Clamp by Biopro, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temporal bone holder.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biopro, Inc.

Sources (1)

  • FDA UDI d5444b1c-bae0-42f1-bdb0-57ad934d9330 33 fields · synced May 30, 2026